0 Evaluaciones

ID

28280

Descripción

Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: End of study contact

Palabras clave

  1. 13/10/17 13/10/17 -
  2. 23/10/17 23/10/17 -
  3. 2/1/18 2/1/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

2 de enero de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0

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    End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

    End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

    End of study contact form
    Descripción

    End of study contact form

    1. Was subject contacted?
    Descripción

    Please select No if continued attempts to contact subject have failed and 3 month EOS period had come to an end. If contact only made with Third party designee instead of subject please complete a THIRD PARTY form.

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0332158 (Contact with)
    SNOMED
    11723008
    UMLS CUI [1,2]
    C0681850 (Study Subject)
    Type of contact
    Descripción

    Type of contact

    Tipo de datos

    integer

    Alias
    UMLS CUI [1]
    C0332158 (Contact with)
    SNOMED
    11723008
    If telephone: Time of contact
    Descripción

    Time of contact

    Tipo de datos

    time

    Alias
    UMLS CUI [1]
    C0805839 (Date last contact)
    LOINC
    MTHU010432
    If telephone: Site staff who conducted call
    Descripción

    ensure documented in source notes

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0302186 (Telephone Call)
    If telephone: Reason why visit was not perfomed in the clinic
    Descripción

    Reason visit was not perfomed in clinic

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0566251 (Reason and justification)
    SNOMED
    288830005
    UMLS CUI [1,2]
    C3838685 (Medical day care clinic)
    SNOMED
    702881000
    Other, specify
    Descripción

    Reason visit was not perfomed in clinic specification

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0566251 (Reason and justification)
    SNOMED
    288830005
    UMLS CUI [1,2]
    C3838685 (Medical day care clinic)
    SNOMED
    702881000

    Similar models

    End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    End of study contact form
    subject contact
    Item
    1. Was subject contacted?
    boolean
    C0332158 (UMLS CUI [1,1])
    C0681850 (UMLS CUI [1,2])
    Item
    Type of contact
    integer
    C0332158 (UMLS CUI [1])
    Code List
    Type of contact
    CL Item
    Clinic visit (1)
    C0008952 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Telephone (2)
    C1515258 (UMLS CUI-1)
    (Comment:en)
    Time of contact
    Item
    If telephone: Time of contact
    time
    C0805839 (UMLS CUI [1])
    Item
    If telephone: Site staff who conducted call
    text
    C0302186 (UMLS CUI [1])
    Code List
    If telephone: Site staff who conducted call
    CL Item
    Physician (34)
    C0031831 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Nurse (35)
    C0028661 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Other (OT)
    C0205394 (UMLS CUI-1)
    (Comment:en)
    Item
    If telephone: Reason why visit was not perfomed in the clinic
    text
    C0566251 (UMLS CUI [1,1])
    C3838685 (UMLS CUI [1,2])
    Code List
    If telephone: Reason why visit was not perfomed in the clinic
    CL Item
    Subject refused (1)
    C1705116 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Subject not able to visit clinic (2)
    C3838685 (UMLS CUI-1)
    C0545082 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Other (OT)
    (Comment:en)
    Reason visit was not perfomed in clinic specification
    Item
    Other, specify
    text
    C0566251 (UMLS CUI [1,1])
    C3838685 (UMLS CUI [1,2])

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